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Is Biopharma Ready for AI? Exploring Tech Strategies Across Large and Small Biopharma

In this GEN webinar, experts from AbbVie and Benchling will share insights into the current tech landscape, AI readiness, and the strategies for digital transformation shaping large and small biopharma.

Integrated Strategies to Accelerate Pre-Clinical Development of Antibody-Drug Conjugates

In this GEN webinar, experts from WuXi AppTec will share essential strategies and methodologies for accelerating pre-clinical assessments of ADCs.

Imaging Large Multiprotein Complexes Using Native Nano-DESI Mass Spectrometry

In this GEN webinar, Dr. Helen Cooper, a leading analytic alchemist from the University of Birmingham, U.K., will discuss improvements in mass spectrometry imaging technology that enable the characterization of the precise protein forms present in multiprotein complexes.

Navigating Quality Control and Release Testing in Cell and Gene Therapy Development

In this GEN webinar, our speakers will present important considerations for quality control testing for biosafety and product characterization in GMP release and stability studies of novel cell and gene therapies.

Mastering the Path: Developing Processes for Successful Clinical-Grade mRNA Manufacturing

In this GEN webinar, we will aim to unlock the secrets behind the iterative process development that ensures the highest standards of mRNA manufacturing.

Using Oxford Nanopore’s Multi-Omic Sequencing to Optimize Plasmids and Vectors for Cell and Gene Therapies

In this GEN webinar, Andrea O’Hara, PhD, a multiomics expert at GENEWIZ from Azenta Life Sciences, will discuss how to use nanopore sequencing technology to enhance the precision and efficiency of cell and gene therapy programs.

Using Patient-Derived Organoids to Develop Novel Therapies for Complex and Inherited Diseases

In this GEN webinar, experts from Xilis and University of Washington and Plurexa will share results from recent research using patient-derived organoids to study multiple myeloma and polycystic kidney disease.

Improving Gene Therapy Design and Manufacturability Using Synthetic Biology and AI

In this GEN webinar, Mark Stockdale will discuss how the application of synthetic biology and artificial intelligence can be used to improve the safety, potency and manufacturability of gene therapies, and introduce AAV Edge, a comprehensive platform for end-to-end gene therapy optimization—from payload design to production cell lines and model-guided processes.

Improved Methods for Characterization of AAV-Based Gene Therapies

On this GEN webinar, experts from Regeneron Pharmaceuticals, Song Nie, PhD, and Tim Tiambeng, PhD, will discuss two novel methods for characterizing AAV-based gene therapy products.

Developing iPSC-Derived Liver Systems for MASLD Modeling and Therapy Screening

In this GEN webinar, Jeremy Tomlinson, PhD, will discuss the pathogenesis of MASLD, share examples from recent research that highlight current progress and advancements in the clinic, and explore the importance of developing efficient pre-clinical models to identify and characterize novel cellular targets associated with disease progression.

Endpoints: Critical Preclinical Markers in Extracellular Protein Degradation Assays

In this GEN webinar, Shyra Gardai, PhD, will demonstrate the potential of the novel extracellular degrading platform, EpiTACs, using the development of bispecific antibodies to degrade the canonical receptor tyrosine kinase epidermal growth factor receptor as a case study

Enhancing Protein Development with Active Learning-Assisted Directed Evolution

In this GEN webinar, Ravi Goel Lal from the Arnold lab at Caltech will present the basics and applications of Active Learning-assisted Directed Evolution (ALDE). He will be joined by Dr. Galit Meshulam-Simon, Associate Director of Commercial Applications at Elegen.